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FDA 510(k)

CLEARVIEW BLOWER/MISTER

K-Number: K973485 · 1997-12-08

ApplicantDlp, Inc.
Decision Date1997-12-08
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CLEARVIEW BLOWER/MISTER is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1997-12-08 under 510(k) number K973485. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARVIEW BLOWER/MISTER?

CLEARVIEW BLOWER/MISTER is a medical device that received FDA 510(k) clearance on 1997-12-08. The listed applicant is Dlp, Inc.. The 510(k) number is K973485.

When did CLEARVIEW BLOWER/MISTER receive FDA 510(k) clearance?

CLEARVIEW BLOWER/MISTER received FDA 510(k) clearance on 1997-12-08, under 510(k) number K973485.

Who is the listed applicant for CLEARVIEW BLOWER/MISTER?

The FDA 510(k) record lists Dlp, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEARVIEW BLOWER/MISTER?

The FDA product code for CLEARVIEW BLOWER/MISTER is FQH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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